Nucleic acid amplification and detection of Mycobacterium species

ABSTRACT

Oligonucleotides used to prime in vitro nucleic acid amplification of 16S rRNA sequences or DNA encoding 16S rRNA sequences for many species within the genus  Mycobacterium  are disclosed. Kits including such oligonucleotides are disclosed. Methods of detecting  Mycobacterium  species using the oligonucleotides in in vitro nucleic acid amplification are disclosed.

RELATED APPLICATIONS

This application is a divisional of U.S. application Ser. No.09/738,274, filed Dec. 15, 2000, and claims the benefit under 35 U.S.C.§119(e) of U.S. Provisional Application No. 60/172,190, filed Dec. 17,1999, the contents of both of which are hereby incorporated byreference.

FIELD OF THE INVENTION

This invention relates to in vitro diagnostic detection of pathogenicbacteria, and specifically relates to compositions and assays fordetecting many species of Mycobacterium by using in vitro nucleic acidamplification and detection of amplified products.

BACKGROUND OF THE INVENTION

Detection of Mycobacterium species in clinical species is important as aclinical diagnostic tool. Historically, M. tuberculosis was thought tobe the only clinically significant pathogen in this genus. A rise in theincidence of drug-resistant strains of M. tuberculosis has furtheremphasized the need to detect this species. Other Mycobacterium species,however, are also clinically important. These are sometimes referred toas “MOTT” for Mycobacterium other than tuberculosis, commonly includingM. avium/intracellulare complex organisms (M. avium, M. intracellulare,M. paratuberculosis, commonly referred to as MAIC), M. gordonae, M.fortuitum, M. chelonae, M. mucogenicum and mixtures of Mycobacteriumspecies in a clinical specimen. For example, fast-growing opportunisticinfections by M. avium complex (MAC) bacteria have been shown to occurfrequently in AIDS and other immunocompromised individuals. In suchinfected individuals, at least 10⁶ MAC cells/ml of sputum sediment havebeen found. Therefore, detection assays that can detect, and optimallydistinguish between, many species of Mycobacterium are clinicallyimportant.

Many clinical methods for detecting and identifying Mycobacteriumspecies in samples require analysis of the bacteria's physicalcharacteristics (e.g., acid-fast staining and microscopic detection ofbacilli), physiological characteristics (e.g., growth on defined media)or biochemical characteristics (e.g., membrane lipid composition). Thesemethods require relatively high concentrations of bacteria in the sampleto be detected, may be subjective depending on the clinical technician'sexperience and expertise, and are time-consuming. Because Mycobacteriumspecies are often difficult to grow in vitro and may take several weeksto reach a useful density in culture, these methods can also result indelayed patient treatment and costs associated with isolating aninfected individual until the diagnosis is completed.

More recently, assays that detect the presence of nucleic acid derivedfrom bacteria in the sample have been preferred because of thesensitivity and relative speed of the assays. In particular, assays thatuse in vitro nucleic acid amplification of nucleic acids present in aclinical sample can provide increased sensitivity and specificity ofdetection. Such assays, however, can be limited to detecting one or afew Mycobacterium species depending on the sequences amplified and/ordetected.

Assays and reagents for detecting Mycobacterium nucleic acid sequenceshave been previously disclosed, for example, in U.S. Pat. Nos.5,554,516, 5,766,849, 5,795,752, 5,906,917, 5,908,744; European PatentNos. EP 0528306 and EP 0818465; and published PCT Patent Applications WO9636733 and WO 9723618.

The present invention provides compositions and relatively simplediagnostic methods that detect a wide spectrum of Mycobacterium speciesthat may be present in a clinical sample.

SUMMARY OF THE INVENTION

According to one aspect of the invention, there is provided a method ofdetecting Mycobacterium species present in a biological sample. Themethod includes the steps of providing a biological sample containingnucleic acid from at least one Mycobacterium species comprising aMycobacterium 16S ribosomal RNA (rRNA) or a DNA encoding theMycobacterium 16S ribosomal rRNA; amplifying the Mycobacterium 16S rRNAor DNA in an in vitro nucleic acid amplification mixture comprising atleast one polymerase activity, and at least two primers having sequencesselected from the group consisting of SEQ ID NO:1 to SEQ ID NO: 34, SEQID NO:37 and SEQ ID NO:38 to produce amplified Mycobacterium nucleicacid;

-   -   and detecting the amplified Mycobacterium nucleic acid by        detecting a label associated with the amplified Mycobacterium        nucleic acid. In one embodiment, the method also includes the        steps of adding to the biological sample at least one capture        oligonucleotide that specifically hybridizes to the        Mycobacterium 16S rRNA and an immobilized nucleic acid that        hybridizes to the capture oligonucleotide under hybridizing        conditions to produce a hybridization complex; and separating        the hybridization complex from other components of the        biological sample before the amplifying step. In preferred        embodiments, the amplifying step amplifies 16S rRNA or DNA of M.        tuberculosis or a Mycobacterium other than tuberculosis (MOTT)        species. In other preferred embodiments, the amplifying step        amplifies 16S rRNA or DNA of M. abscessus, M. africanum, M.        asiaticum, M. avium, M. bovis, M. celatum, M. chelonae, M.        flavescens, M. fortuitum, M. gastri, M. gordonae, M.        haemophilum, M. intracellulare, M. interjectum, M.        intermedium, M. kansasii, M. malmoense, M. marinum, M.        non-chromogenicum, M. paratuberculosis, M. phlei, M.        scrofulaceum, M. shimodei, M. simiae, M. smegmatis, M.        szulgai, M. terrae, M. triviale, M. tuberculosis, M. ulcerans        or M. xenopi. In another embodiment, the detecting step uses at        least one probe that hybridizes specifically to the amplified        Mycobacterium nucleic acid. The detecting step may use at least        one labeled probe that hybridizes specifically to the amplified        Mycobacterium nucleic acid or may use a plurality of probes that        hybridize specifically to the amplified Mycobacterium nucleic        acid. In preferred embodiments, the amplifying step uses a        combination of at least a first primer and a second primer,        wherein the first primer is selected from the group consisting        of SEQ ID NO:1 to SEQ ID NO:12, and the second primer is        selected from the group consisting of SEQ ID NO:13 to SEQ ID        NO:34, SEQ ID NO:37 and SEQ ID NO:38. Additional embodiments in        the amplifying step use a combination of at least a first primer        and a second primer, wherein the first primer is selected from        the group consisting of SEQ ID NO:7 to SEQ ID NO:12, and the        second primer is selected from the group consisting of SEQ ID        NO:13 to SEQ ID NO:34, SEQ ID NO:37 and SEQ ID NO:38. Preferred        combinations of first and second primer used in the amplifying        step are: the first primer has the sequence of SEQ ID NO:7, and        the second primer has the sequence of SEQ ID NO:13; the first        primer has the sequence of SEQ ID NO:7, and the second primer        has the sequence of SEQ ID NO:14; the first primer has the        sequence of SEQ ID NO:7, and the second primer has the sequence        of SEQ ID NO:15; the first primer has the sequence of SEQ ID        NO:7, and the second primer has the sequence of SEQ ID NO:16;        the first primer has the sequence of SEQ ID NO:8, and the second        primer has the sequence of SEQ ID NO:13; the first primer has        the sequence of SEQ ID NO:8, and the second primer has the        sequence of SEQ ID NO:14; the first primer has the sequence of        SEQ ID NO:8, and the second primer has the sequence of SEQ ID        NO:15; the first primer has the sequence of SEQ ID NO:9, and the        second primer has the sequence of SEQ ID NO:13; the first primer        has the sequence of SEQ ID NO:9, and the second primer has the        sequence of SEQ ID NO:14; the first primer has the sequence of        SEQ ID NO:9, and the second primer has the sequence of SEQ ID        NO:15; the first primer has the sequence of SEQ ID NO:10, and        the second primer has the sequence of SEQ ID NO:16; the first        primer has the sequence of SEQ ID NO:11, and the second primer        has the sequence of SEQ ID NO:13; the first primer has the        sequence of SEQ ID NO:11, and the second primer has the sequence        of SEQ ID NO:16; the first primer has the sequence of SEQ ID        NO:11, and the second primer has the sequence of SEQ ID NO:17;        the first primer has the sequence of SEQ ID NO:11, and the        second primer has the sequence of SEQ ID NO:18; the first primer        has the sequence of SEQ ID NO:11, and the second primer has the        sequence of SEQ ID NO:19; the first primer has the sequence of        SEQ ID NO:11, and the second primer has the sequence of SEQ ID        NO:20; or the first primer has the sequence of SEQ ID NO:12, and        the second primer has the sequence of SEQ ID NO:15. In one        embodiment, the amplifying step uses a combination of at least a        first primer and a second primer, wherein the first primer has        the sequence of SEQ ID NO:11, and the second primer has the        sequence of SEQ ID NO:16, SEQ ID NO:30 or SEQ ID NO:37. In        another embodiment, the amplifying step uses a combination of a        first primer having the sequence of SEQ ID NO:11, and two second        primers, one second primer having the sequences SEQ ID NO:16 and        the other second primer having the sequence of SEQ ID NO:37.

Another aspect of the invention is a composition for amplifying in an invitro amplification reaction a Mycobacterium 16S rRNA sequence or a DNAencoding the Mycobacterium 16S rRNA, comprising one or moreoligonucleotides having a base sequence selected from the groupconsisting of SEQ ID NO:1 to SEQ ID NO: 34, SEQ ID NO:37 and SEQ IDNO:38. In preferred embodiments, the composition includes at least onefirst oligonucleotide containing the sequence of any one of SEQ ID NO:1to SEQ ID NO:12, and at least one second oligonucleotide containing thesequence of any one of SEQ ID NO:13 to SEQ ID NO:34, SEQ ID NO:37 or SEQID NO:38. In another embodiment, the composition includes at least onefirst oligonucleotide containing the sequence of any one of SEQ ID NO:7to SEQ ID NO:12, and at least one second oligonucleotide containing thesequence of any one of SEQ ID NO:13 to SEQ ID NO:34, SEQ ID NO:37 or SEQID NO:38.

Another aspect of the invention is a kit containing any of theoligonucleotides having a base sequence selected from the groupconsisting of SEQ ID NO:1 to SEQ ID NO: 34, SEQ ID NO:37 and SEQ IDNO:38. In preferred embodiments, the kit includes at least one firstoligonucleotide containing the sequence of any one of SEQ ID NO:1 to SEQID NO:12, and at least one second oligonucleotide containing thesequence of any one of SEQ ID NO:13 to SEQ ID NO:34, SEQ ID NO:37 or SEQID NO:38. In another embodiment, the kit includes at least one firstoligonucleotide containing the sequence of any one of SEQ ID NO:7 to SEQID NO:12, and at least one second oligonucleotide containing thesequence of any one of SEQ ID NO:13 to SEQ ID NO:34, SEQ ID NO:37 or SEQID NO:38.

DETAILED DESCRIPTION

The present invention includes methods of detecting Mycobacteriumnucleic acids, specifically 16S rRNA sequences, present in biologicalsamples derived from humans, preferably in processed sputum samples. Thepresent invention also includes compositions which include nucleic acidoligomers (“capture oligonucleotides”) used to specifically captureMycobacterium 16S rRNA sequences present in a biological sample,amplification nucleic acid oligomers (“primers”) used to specificallyamplify selected portions of the captured 16S rRNA sequences and nucleicacid oligomers (“probes” or “labeled probes”) for detecting amplifiedMycobacterium sequences.

The nucleic acid sequences of this invention are useful for capturing,amplifying and detecting Mycobacterium nucleic acid present in abiological sample containing any of a variety of Mycobacterium species.The methods of the present invention are valuable for detectingMycobacterium nucleic acid in a biological sample, and thus areimportant for diagnosis of infection that might result from a number ofMycobacterium species. These methods are especially important forscreening for opportunistic infections by MOTT species, or M.tuberculosis infections.

To aid in understanding terms used in describing the invention, thefollowing definitions are provided.

By “biological sample” is meant any tissue or material derived from aliving or dead human which may contain Mycobacterium nucleic acid.Samples include, for example, sputum, respiratory tissue or exudates,peripheral blood, plasma or serum, cervical swab samples, biopsy tissue,gastrointestinal tissue, urine, feces, semen or other body fluids,tissues or materials. Samples also include bacterial cultures (liquid oron a solid media) and environmental samples. The biological sample maybe treated to physically disrupt tissue or cell structure, thusreleasing intracellular components into a solution which may furthercontain enzymes, buffers, salts, detergents and the like which are usedto prepare the sample for analysis.

By “nucleic acid” is meant a multimeric compound comprising nucleosidesor nucleoside analogs which have nitrogenous heterocyclic bases, or baseanalogs, where the nucleosides are covalently linked via a backbonestructure to form a polynucleotide. Conventional ribonucleic acid (RNA)and deoxyribonucleic acid (DNA) are included in the term “nucleic acid”as are analogs thereof. A nucleic acid backbone may comprise a varietyof linkages known in the art, including one or more ofsugar-phosphodiester linkages, peptide-nucleic acid bonds (referred toas “peptide nucleic acids”; Hydig-Hielsen et al., PCT Int'l Pub. No. WO95/32305), phosphorothioate linkages, methylphosphonate linkages orcombinations thereof. Sugar moieties of the nucleic acid may be eitherribose or deoxyribose, or similar compounds having known substitutions,e.g., 2′ methoxy substitutions and/or 2′ halide substitutions.Nitrogenous bases may be conventional bases (A, G, C, T, U), knownanalogs thereof (e.g., inosine or others; see The Biochemistry of theNucleic Acids 5-36, Adams et al., ed., 11^(th) ed., 1992), or knownderivatives of purine or pyrimidine bases (see, Cook, PCT Int'l Pub. No.WO 93/13121) and “abasic” residues in which the backbone includes nonitrogenous base for one or more residues (Arnold et al., U.S. Pat. No.5,585,481). A nucleic acid may comprise only conventional sugars, basesand linkages, as found in RNA and DNA, or may include both conventionalcomponents and substitutions (e.g., conventional bases linked via amethoxy backbone, or a nucleic acid including conventional bases and oneor more base analogs).

By “oligonucleotide” or “oligomer” is meant a nucleic acid havinggenerally less than 1,000 residues, including polymers in a size rangehaving a lower limit of about 2 to 5 nucleotide residues and an upperlimit of about 500 to 900 nucleotide residues. Preferred oligomers arein a size range having a lower limit of about 5 to about 15 residues andan upper limit of about 50 to 600 residues; more preferably, in a sizerange having a lower limit of about 10 residues and an upper limit ofabout 100 residues. Oligomers may be purified from naturally occurringsources, but preferably are synthesized using well known methods.

By “amplification oligonucleotide” or “amplification oligomer” is meantan oligonucleotide that hybridizes to a target nucleic acid, or itscomplement, and participates in an in vitro nucleic acid amplificationreaction (e.g., primers and promoter primers). Preferably, anamplification oligonucleotide contains at least about 10 contiguousbases, and more preferably at least about 12 contiguous bases, which arecomplementary to a region of the target nucleic acid sequence (or acomplementary strand thereof). The contiguous bases are preferably atleast 80%, more preferably at least 90% complementary to the sequence towhich the amplification oligonucleotide binds. An amplificationoligonucleotide is preferably about 10 to about 60 bases long and mayinclude modified nucleotides or base analogs.

Amplification oligonucleotides and oligomers may be referred to as“primers” or “promoter-primers.” A “primer” refers to an oligonucleotidewhich is capable of hybridizing to a template nucleic acid and which hasa 3′ end that is extended in a polymerization reaction, usually mediatedby an enzyme. The 5′ region of the primer may be non-complementary tothe target nucleic acid and include additional bases, such as a promotersequence. Such a primer is referred to as a “promoter-primer.” Thoseskilled in the art will appreciate that any oligomer that can functionas a primer can be modified to include a 5′ promoter sequence, and thuscould function as a promoter primer. Similarly, any promoter primer canserve as a primer, independent of its promoter sequence function.

By “amplification” is meant any known in vitro procedure for obtainingmultiple copies of a target nucleic acid sequence or its complement orfragments thereof. In vitro amplification refers to production of anamplified nucleic acid that may contain less than the complete targetregion sequence or its complement. Known amplification methods include,for example, transcription-mediated amplification, replicase-mediatedamplification, polymerase chain reaction (PCR) amplification, ligasechain reaction (LCR) amplification and strand-displacement amplification(SDA). Replicase-mediated amplification uses self-replicating RNAmolecules, and a replicase such as QB-replicase (Kramer et al., U.S.Pat. No. 4,786,600; PCT Int'l Pub. No. WO 90/14439). PCR amplificationis well known and uses DNA polymerase, primers and thermal cycling tosynthesize multiple copies of the two complementary strands of DNA orcDNA (Mullis et al., U.S. Pat. Nos. 4,683,195, 4,683,202, and 4,800,159;Methods in Enzymology, 1987, Vol. 155: 335-350). LCR amplification usesat least four separate oligonucleotides to amplify a target and itscomplementary strand by using multiple cycles of hybridization,ligation, and denaturation (EP Pat. App. Pub. No. 0 320 308). SDA is amethod in which a primer contains a recognition site for a restrictionendonuclease such that the endonuclease will nick one strand of ahemimodified DNA duplex that includes the target sequence, followed byamplification in a series of primer extension and strand displacementsteps (Walker et al, 1992, Proc. Natl. Acad. Sci. USA 89:392-396; andU.S. Pat. No. 5,422,252). Transcription-mediated amplification is apreferred embodiment of the present invention. Those skilled in the artwill understand that the oligonucleotide primer sequences of the presentinvention may be readily used in any in vitro amplification method basedon primer extension by a polymerase.

By “transcription-mediated amplification” or “transcription-associatedamplification” is meant any type of nucleic acid amplification that usesan RNA polymerase to produce multiple RNA transcripts from a nucleicacid template. Transcription-mediated amplification (“TMA”) generallyemploys an RNA polymerase activity, a DNA polymerase activity,deoxyribonucleoside triphosphates, ribonucleoside triphosphates, and apromoter primer and a second non-promoter primer, and optionally mayinclude one or more additional oligonucleotides (sometimes referred toas “helpers”). Transcription-associated amplification methods are wellknown in the art, as disclosed in detail elsewhere (Kacian et al., U.S.Pat. Nos. 5,399,491 and 5,554,516; Kacian et al., PCT Int'l Pub. No. WO93/22461; Burg et al., U.S. Pat. No. 5,437,990; Gingeras et al., PCTInt'l Pub. Nos. WO 88/01302 and WO 88/10315; Malek et al., U.S. Pat. No.5,130,238; Urdea et al., U.S. Pat. Nos. 4,868,105 and 5,124,246;McDonough et al., PCT Int'l Pub. No. WO 94/03472; and Ryder et al., PCTInt'l Pub. No. WO 95/03430). Preferred transcription-mediatedamplification methods of the present invention are those disclosed byKacian et al. (U.S. Pat. Nos. 5,399,491 and 5,554,516; PCT ApplicationNo. WO 93/22461).

By “probe” is meant a nucleic acid oligomer that hybridizes specificallyto a target sequence in a nucleic acid or its complement, preferably inan amplified nucleic acid, under conditions that promote hybridization,thereby allowing detection of the target sequence or amplified nucleicacid. Detection may either be direct (i.e., resulting from a probehybridizing directly to the target sequence or amplified nucleic acid)or indirect (i.e., resulting from a probe hybridizing to an intermediatemolecular structure that links the probe to the target sequence oramplified nucleic acid). A probe's “target” generally refers to asequence within (i.e., a subset of) an amplified nucleic acid sequencewhich hybridizes specifically to at least a portion of a probe oligomerusing standard hydrogen bonding (i.e., base pairing). Sequences that are“sufficiently complementary” allow stable hybridization of a probeoligomer to a target sequence, even if the two sequences are notcompletely complementary. A probe may be labeled or unlabeled, dependingon the method of detection used.

By “sufficiently complementary” is meant a contiguous nucleic acid basesequence that is capable of hybridizing to another base sequence byhydrogen bonding between a series of complementary bases. Complementarybase sequences may be complementary at each position in sequence usingstandard base pairing (e.g., G:C, A:T or A:U pairing) or may contain oneor more residues that are not complementary using standard hydrogenbonding (including abasic residues), but in which the entirecomplementary base sequence is capable of specifically hybridizing withanother base sequence in appropriate hybridization conditions.Contiguous bases are preferably at least about 80%, more preferably atleast about 90% complementary to a sequence to which an oligomerspecifically hybridizes. Appropriate hybridization conditions are wellknown to those skilled in the art, can be predicted readily based onsequence composition and conditions, or can be determined empirically byusing routine testing (see Sambrook et al., Molecular Cloning, ALaboratory Manual, 2^(nd) ed. (Cold Spring Harbor Laboratory Press, ColdSpring Harbor, N.Y., 1989) at §§ 1.90-1.91, 7.37-7.57, 9.47-9.51 and11.47-11.57, particularly at §§ 9.50-9.51, 11.12-11.13, 11.45-11.47 and11.55-11.57).

By “capture oligonucleotide” or “capture oligomer” is meant at least onenucleic acid oligomer that provides means for specifically joining atarget sequence and an immobilized oligomer based on base pairhybridization (see PCT Application WO 98/50583). Generally, a captureoligomer includes two binding regions: a target-specific binding regionand an immobilized probe-specific binding region Sometimes, a captureoligomer is referred to as a “capture probe.”

By “immobilized probe” or “immobilized nucleic acid” is meant a nucleicacid that joins, directly or indirectly, a capture oligomer to a solidsupport. An immobilized probe is an oligomer joined to a solid supportthat facilitates separation of bound target sequence from unboundmaterial in a sample. Any known solid support may be used, such asmatrices and particles free in solution, made of any known material(e.g., nitrocellulose, nylon, glass, polyacrylate, mixed polymers,polystyrene, silane polypropylene and metal particles, preferablyparamagnetic particles). Preferred supports are monodisperseparamagnetic spheres (i.e., uniform in size±about 5%), thereby providingconsistent results, to which an immobilized probe is stably joineddirectly (e.g., via a direct covalent linkage, chelation, or ionicinteraction), or indirectly (e.g., via one or more linkers), permittinghybridization to another nucleic acid in solution.

By “separating” or “purifying” is meant that one or more components ofthe biological sample are removed from one or more other components ofthe sample. Sample components include nucleic acids in a generallyaqueous solution which may also include other materials (e.g., proteins,carbohydrates, lipids and/or nucleic acids). Preferably, a separating orpurifying step removes at least about 70%, more preferably at leastabout 90% and, even more preferably, at least about 95% of the othercomponents present in the sample.

By “label” is meant a molecular moiety or compound that can be detectedor can lead to a detectable response. A label is joined, directly orindirectly, to a nucleic acid probe or to the nucleic acid to bedetected (e.g., amplified product). Direct labeling can occur throughbonds or interactions that link the label to the probe (e.g., covalentbonds or non-covalent interactions). Indirect labeling can occur throughuse of a bridging moiety or “linker”, such as additionaloligonucleotide(s), which is either directly or indirectly labeled.Bridging moieties can be used to amplify a detectable signal. Labels canbe any known detectable moiety (e.g., a radionuclide, ligand such asbiotin or avidin, enzyme or enzyme substrate, reactive group, orchromophore, such as a dye or colored particle, luminescent compond,including bioluminescent, phosphorescent or chemiluminescent compounds,and fluorescent compound). Preferably, the label on a labeled probe thatis detectable in a homogeneous assay system (i.e., in a mixture, boundlabeled probe exhibits a detectable change compared to unbound labeledprobe). A preferred label for use in a homogenous assay is achemiluminescent compound (see U.S. Pat. Nos. 5,656,207, 5,658,737 and5,639,604), more preferably an acridinium ester (“AE”) compound, such asstandard AE or derivatives thereof. Methods of attaching labels tonucleic acids and detecting labels are well known in the art (e.g., seeSambrook et al., Molecular Cloning, A Laboratory Manual, 2^(nd) ed.(Cold Spring Harbor Laboratory Press, Cold Spring Habor, N.Y., 1989),Chapter 10; U.S. Pat. No. 5,658,737, U.S. Pat. Nos. 5,656,207,5,547,842, 5,283,174 and 4,581,333; and European Pat. App. No. 0 747706).

A “homogeneous detectable label” refers to a label whose presence can bedetected in a homogeneous fashion based upon whether the label is on aprobe hybridized to a target sequence. That is, a homogeneous detectablelabel can be detected without physically removing hybridized fromunhybridized forms of the label or labeled probe. Homogeneous detectablelabels and methods of detecting them have been previously described indetail (U.S. Pat. Nos. 5,283,174, 5,656,207 and 5,658,737).

By “consisting essentially of” is meant that additional component(s),composition(s) or method step(s) that do not materially change the basicand novel characteristics of the present invention may be included inthe compositions or kits or methods of the present invention. Suchcharacteristics include the ability to detect Mycobacterium species rRNAsequences and/or DNA sequences encoding the rRNA in a biological sampleat a copy number of about 100 or more per sample. Any component(s),composition(s), or method step(s) that have a material effect on thebasic characteristics of the present invention would fall outside ofthis term.

Unless defined otherwise, all scientific and technical terms used hereinhave the same meaning as commonly understood by those skilled in therelevant art. General definitions of many of the terms used herein areprovided, for example, in Dictionary of Microbiology and MolecularBiology, 2nd ed. (Singleton et al., 1994, John Wiley & Sons, New York,N.Y.) or The Harper Collins Dictionary of Biology (Hale & Marham, 1991,Harper Perennial, New York, N.Y.). Unless mentioned otherwise, thetechniques employed or contemplated herein are standard methodologieswell known to one of ordinary skill in the art.

The present invention includes compositions (nucleic acid captureoligomers, amplification oligomers and probes) and methods for detectingMycobacterium species nucleic acid in a human biological sample. Toselect DNA sequences appropriate for use as capture oligomers, primersand probes, known rRNA or the corresponding genomic sequences from M.tuberculosis, and MOTT species, such as M. celatum and M. xenopi,including partial or complementary sequences, available from publiclyaccessible databases (e.g., GenBank) were aligned by matching regions ofthe same or similar sequences and compared using well known molecularbiology techniques. Although sequence comparisons may be facilitated byusing algorithms, those skilled in the art can readily perform suchcomparisons manually and visually. Portions of sequences containingrelatively few sequence variants between the compared sequences werechosen as a basis for designing synthetic oligomers suitable for use incapture, amplification and detection of amplified sequences. Otherconsiderations in designing oligomers included the relative GC contentof the sequence (ranging from about 30-55%) and the relative absence ofpredicted secondary structure (e.g., hairpin structures) within asequence, all well known in the art. Based on these analyses, theoligomers having sequences of SEQ ID NO:1 to SEQ ID NO:35 were designedand synthesized.

Target capture is preferably included in the method to increase theconcentration or purity of the target nucleic acid before in vitroamplification. Preferably, target capture involves a relatively simplemethod of hybridizing and isolating the target nucleic acid, asdescribed in detail in PCT Patent Application WO 98/50583. Briefly, anoligonucleotide attached to a solid support is put in contact with amixture containing the target nucleic acid under appropriatehybridization conditions to allow the target nucleic acid to bereleasably attached to the solid support. Target capture may result fromdirect hybridization between the target nucleic acid and theoligonucleotide attached to the solid support, or may be indirectly withone or more oligonucleotides forming a hybridization complex that linksthe target nucleic acid to the oligonucleotide attached to the solidsupport. The solid support is preferably a particle that can be readilyseparated from the solution, more preferably a paramagnetic particlethat can be retrieved by applying a magnetic field to the vessel. Then,the target nucleic acid linked to the solid support is washed andamplified upon exposure to the appropriate primers, substrates andenzymes in an in vitro amplification reaction.

Generally, for capture oligomer sequences, the oligomer includes asequence that specifically binds to the target sequence and a “tail”sequence used in capturing the complex to an immobilized sequence (e.g.,T₁₄ oligomer) on the solid support. That is, the capture oligomerincludes a sequence that binds specifically to Mycobacterium rRNAsequence which is covalently attached to a 3′ tail sequence (e.g., apoly-A sequence complementary to the immobilized sequence). Any backboneto linking the base sequence of a capture oligomer may be used, butpreferably the capture oligomer backbone includes O-methoxy linkages.The tail sequence (preferably 5-50 nt long) hybridizes to an immobilizedcomplementary sequence to purify the hybridized target nucleic acid fromthe other sample components. A preferred capture oligomer has thesequence of SEQ ID NO:35 (CTAGTCTGCCCGTATTTT(A)₃₀).

Amplifying the captured target region using at least two primers can beaccomplished using a variety of known nucleic acid amplificationreactions, but preferably uses a transcription-associated amplificationreaction. Using such an in vitro amplification method, many strands ofnucleic acid are produced from a single copy of target nucleic acid,thus permitting detection of the target by specifically binding theamplified sequences to one or more detecting probes.Transcription-associated amplification has been described in detailelsewhere (Kacian et al., U.S. Pat. Nos. 5,399,491 and 5,554,516).Preferably, transcription-associated amplification uses two-types ofprimers (one referred to as a promoter-primer because it contains apromoter sequence for an RNA polymerase), two enzymes (a reversetranscriptase and an RNA polymerase), substrates (deoxyribonucleosidetriphosphates, ribonucleoside triphosphates) and appropriate salts andbuffers in solution to produce multiple RNA transcripts from a nucleicacid template. Briefly, in the first step, a promoter-primer hybridizesspecifically to a target RNA sequence and reverse transcriptase createsa first strand cDNA by extension from the 3′ end of the promoter-primer.Making the cDNA available for hybridization with the second primer maybe achieved by using techniques well known in the art, such as, bydenaturing the duplex or using RNase H activity. Preferably, RNase Hactivity supplied by the reverse transcriptase degrades the RNA in theresulting DNA:RNA duplex. A second primer then binds to the cDNA and anew strand of DNA is synthesized from the end of the second primer usingthe reverse transcriptase, to create a double-stranded DNA having afunctional promoter sequence at one end. The RNA polymerase binds to thedouble-stranded promoter sequence and transcription produces multipletranscripts or “amplicons.” These amplicons then are used in thetranscription-associated amplification process, each serving as atemplate for a new round of replication, thus generating large amountsof single-stranded amplified nucleic acid (about 100 to about 3,000copies of RNA transcripts synthesized from a single template).Preferably, amplification uses substantially constant reactionconditions (i.e., is substantially isothermal).

Primer sequences (SEQ ID NO:1 to SEQ ID NO:34, SEQ ID NO:37) bindspecifically to a target sequence or a complement of a target sequence,although primer sequences may contain sequences that do not bind to thetarget sequence or its complement. In particular, T7 promoter primers(SEQ ID NO:7 to SEQ ID NO:12) include a T7 promoter sequence (shownseparately in SEQ ID NO:36) attached to the portion of the primersequence that binds to the target or its complement. Those skilled inthe art will appreciate that a target-specific primer sequence, with orwithout an attached promoter sequence (SEQ ID NO:1 to SEQ ID NO:6), maybe useful as a primer in a variety of in vitro amplification conditions.

Preferred methods of the present invention are described in the examplesthat follow. Briefly, the assays include the steps of providing abiological sample containing the target Mycobacterium rRNA, targetcapture of the rRNA, in vitro nucleic acid amplification and detectionof the amplified nucleic acid products. In preferred embodiments thatuse transcription-mediated amplification (TMA), the final amplificationmixture includes the captured target rRNA, at least one T7 promoterprimer that includes a target-specific sequence and a T7 promotersequence, at least one second (non-T7) primer that hybridizesspecifically to a first strand cDNA made from the target using the T7promoter primer, and substrates and cofactors for enzymaticpolymerization by reverse transcriptase and T7 RNA polymerase in themixture. The captured target rRNA does not have to be separated from thesolid support for use in the TMA reaction. The T7 promoter sequence,when double-stranded, serves as a functional promoter for T7 RNApolymerase to produce multiple transcripts. The amplified products maybe detected using any of a variety of known methods, includinghybridizing the amplified products, or portions thereof, to acomplementary probe sequence. The probe which includes a sequence thathybridizes specifically to a portion of the target region that isamplified using the two amplification oligonucleotides. In someembodiments, a labeled probe is used to detect the amplified products,whereas in other embodiments, the amplified products are labeled andhybridized to immobilized probes, preferably many probes present in anarray. The complex of the probe and the hybridized amplified product isthen detected.

More specifically, a typical assay used the following steps andconditions.

A sample (e.g., 0.5 ml of sputum sediment or bacterial culture, forpositive control reactions, an equal volume of water or buffercontaining a known amount of rRNA) was mixed with an equal volume of a2× lysis buffer (e.g., 20 mM HEPES, 0.5% (w/v) lithium lauryl sulfate,pH 8) in a tube. To release nucleic acids from the bacteria, the mixturewas vortexed in the presence of glass beads, or sonicated for 15 min,and then organisms remaining unlysed were heat killed by incubating at95° C. for 15 min.

Generally 250 μl of the lysate was used in the target capture step in anew tube. To capture the target rRNA, the mixture included 250 μl ofprepared sample, 250 μl of a target capture solution containing 5 pmolsof SEQ ID NO:35, and 50 μg of paramagnetic particles (0.7-1.05μparticles, Seradyn, Indianapolis, Ind.) with attached immobilizedpoly-dT₁₄ probe. Immobilized probes were attached using standardcarbodiimide chemistry methods (Lund, et al., 1988, Nuc. Acids Res.16:10861-10880). The target capture mixture was heated at 60° C. forabout 20 min and then cooled to room temperature to allow hybridization.A magnetic field was applied for 5 min to attract the magnetic particleswith the attached complex containing the target RNA to a location on thereaction container (substantially as described in U.S. Pat. No.4,895,650). The particles were then washed twice with 1 ml of a washingbuffer (10 mM HEPES, 6.5 mM NaOH, 1 mM EDTA, 150 mM NaCl, 0.1% (w/v)sodium lauryl sulfate) by resuspending the particles in the buffer andthen repeating the magnetic separation step.

For transcription mediated amplification, performed substantially asdescribed previously (Kacian et al., U.S. Pat. Nos. 5,399,491 and5,554,516), washed particles were suspended in 75 μl of amplificationreagent solution (1.1 mM rUTP, 4 mM rATP, 2.7 mM rCTP, 6.7 mM rGTP, 0.67mM each dNTP, 13.3 mM KCl, 47 mM Tris, 17.1 mM MgCl) and at least twoprimer oligomers (at least one promoter primer and a second primer,usually at 0.08 μM final concentration), and covered with a layer (200μl) of inert oil to prevent evaporation. The mixture was incubated at42° C. for 5 min, and then 25 μl of enzyme reagent was added (containing2800 U of MMLV reverse transcriptase and 2000 U of T7 RNA polymerase perreaction, in a buffer containing 50 mM HEPES, 1 mM EDTA, 10% (v/v)Triton™ X-100, 120 mM KCl, 20% (v/v) glycerol). The mixture was shakengently and further incubated at 42° C. for 1 hr. Negative controlsconsisted of all of the same reagents but substituting an equal volumeof water or buffer that contained no target nucleic acid.

Amplified Mycobacterium sequences were detected, in some cases, using anacridinium ester (AE)-labeled probe which was detected bychemiluminescence in a suitable luminometer (e.g., LEADER™ luminometer,Gen-Probe Incorporated, San Diego, Calif.) and expressed in relativelight units (RLU) substantially as described previously (U.S. Pat. No.5,658,737 at column 25, lines 27-46; Nelson et al., 1996, Biochem.35:8429-8438 at 8432). Generally, the average (mean) of detected RLU forreplicate assays are reported. The probes were: for M. tuberculosisdetection, SEQ ID NO:39 (GTCTTGTGGTGGAAAGCGCTTTAG), for M. aviumdetection, SEQ ID NO:40 (GGACCTCAAGACGCATGTC), for M. xenopi detection,SEQ ID NO:41 (TAGGACCATTCTGCGCATGTG), and for M. gastri and M. kansasii,SEQ ID NO:42 (TAGGACCACTTGGCGCATGCC).

In other cases, the amplified sequences were detected on an immobilizedarray of DNA probes specific for detection of Mycobacterium sequences,as described in detail previously (A. Troesch et al, 1999, J. Clin.Microbiol. 37(1): 49-55). The analysis was perfomed on the GeneChip™instrumentation system (Affymetrix, Santa Clara, Calif.) to detect theintensity and pattern of fluorescent signals (expressed as relativefluorescence units or RFU) on the hybridized array. This systemcomprises a GeneChip™ fluidics station and the GeneArray™ scanner(Hewlett-Packard, Palo Alto, Calif.) and GeneChip™ analysis software, analgorithm to determine nucleotide base calling and determine the nucleicacid sequence present in the amplified nucleic acid. The systemgenerates a report of the most likely Mycobacterium species present.

The following non-limiting examples demonstrate aspects of preferredembodiments of the present invention.

EXAMPLE 1 In Vitro Amplification of M. tuberculosis rRNA Using DifferentPrimer Combinations

Using the amplification and labeled probe detection methods describedabove, the efficiencies of transcription-mediated amplification usingdifferent combinations of T7 promoter primers and second primers weretested. The target sequences for these assays were synthetic transcriptsof M. tuberculosis rRNA sequences, provided at 10², 10³ or 10⁶ copiesper in vitro amplification reaction. Amplification was assessed based onthe detected RLU. Table 1 presents the results obtained with thesecombinations of amplification oligonucleotides for the amount of targetcopies provided, shown in parentheses for each RLU result presented.Each result represents a single assay. TABLE 1 Detected RLU followingamplification of M. tuberculosis rRNA (10², 10³ or 10⁶ copies/reaction)Second Primer Promoter Primer SEQ ID NO: 15 SEQ ID NO: 13 SEQ ID NO: 14SEQ ID NO: 16 SEQ ID NO: 8 2.5 × 10⁶ (10⁶) 0.7 × 10⁶ (10³) 0.8 × 10⁵(10³) Not Tested 2.2 × 10⁵ (10³) 4.5 × 10⁵ (10³) SEQ ID NO: 7 3.2 × 10⁶(10⁶) 2.4 × 10⁶ (10³) 2.0 × 10⁶ (10³) 3.2 × 10⁶ (10³) 3.0 × 10⁶ (10³)1.0 × 10⁶ (10³) 1.2 × 10⁶ (10²) SEQ ID NO: 9 1.5 × 10⁶ (10⁶) 0.4 × 10⁶(10³) 0.7 × 10⁶ (10³) Not Tested 1.3 × 10⁶ (10³) 0.8 × 10⁶ (10³) SEQ IDNO: 12 1.4 × 10⁶ (10⁶) Not Tested Not Tested Not Tested SEQ ID NO: 10Not Tested Not Tested Not Tested 0.8 × 10⁶ (10²) SEQ ID NO: 11 NotTested Not Tested Not Tested 0.8 × 10⁶ (10²)

Signals of 5×10⁴ or greater RLU are considered positive. Thus, theseresults show that all of the tested combinations of promoter primers andprimers amplified the target Mycobacterium sequence, with as few as 102copies of target present in the reaction.

EXAMPLE 2 In Vitro Amplification of Mycobacterium Species UsingCombinations of Primers

Using similar amplification and detection methods as described above andin Example 1, various combinations of T7 promoter primers and non-T7second primers were tested using target 16S rRNA isolated from a varietyof Mycobacterium species (M. tuberculosis, M. bovis, M. avium, M.gastri, M. intracellulare, M. scrofulaceum, M. xenopi and M. kansasii).The bacteria were obtained from the American Type Culture Collection(ATCC, Manassas, Va.) or the “DSM” culture collection (see Table 2 foraccession numbers) and grown in vitro using standard microbiologymethods.

In one set of experiments, the target capture and amplificationreactions were performed using about 10⁴ lysed bacteria per reaction(equivalent to about 10⁷ copies of rRNA per reaction). The amplificationreactions used a T7 promoter primer of SEQ ID NO:11) and a non-T7 secondprimer of SEQ ID NO:16. The RLU results obtained for the amplificationproducts for each species of target are shown in Table 2. These resultsshow that a single combination of two primer sequences can amplify 16SrRNA target sequences from many species of Mycobacterium (the sourcereference number for each species tested is shown in parentheses).Results of 5×10⁴ or greater RLU are considered positive. TABLE 2 RLUDetected for Mycobacterium species Target Sequences Amplified Using SEQID NO: 11 and SEQ ID NO: 16 Target 16S rRNA Source Detected RLU M.tuberculosis (ATCC 27294) 4.0 × 10⁶ M. bovis (ATCC 19274) 4.2 × 10⁶ M.avium (DSM 43216) 1.8 × 10⁶ M. intracellulare (ATCC 15985) 7.5 × 10⁶ M.kansasii (DSM 43224) 2.5 × 10⁶ M. gastri (ATCC 15754) 2.7 × 10⁶ M.xenopi (ATCC 19250) 1.0 × 10⁶ M. scrofulaceum (ATCC 19981) 2.8 × 10⁶

To further demonstrate that primers of the present invention are notspecies-limited for amplification in vitro, additional combinations ofT7 promoter primers and non-T7 second primers were similarly tested butusing different amounts of target per reaction. In these assays, the T7promoter primer had the sequence of SEQ ID NO:11, and was combined withsecond primers having the sequences of SEQ ID NO:13, SEQ ID NO:17, SEQID NO:18, SEQ ID NO:19 or SEQ ID NO:20. The results are shown in Table3. These results show that different combinations of promoter primer andsecond primers can also amplify 16S rRNA sequences from a variety ofMycobacterium species. TABLE 3 RLU Detected for Mycobacterium speciesTarget Sequences Amplified Using SEQ ID NO: 11 and Different SecondPrimers Target Source Second Primers (SEQ ID NO) Copies/reaction NO: 13NO: 17 NO: 18 NO: 19 NO: 20 M. tuberculosis 10⁵ <10⁶ 2.7 × 10⁶ 2.1 × 10⁶2.7 × 10⁶ Not tested 10² Not tested 1.2 × 10⁶ 4.0 × 10⁵ 2.5 × 10⁵ Nottested M. intracellulare 10⁵ 4.0 × 10⁵ 2.3 × 10⁶ Not tested 5.0 × 10⁵Not tested M. xenopi 10⁵ Not tested 3.0 × 10⁴ Not tested Not tested 3.0× 10⁶ M. kansasii 10⁵ Not tested Not tested <10⁴ Not tested Not tested

EXAMPLE 3 In Vitro Amplification of Mycobacterium Species UsingDifferent Non-T7 Second Primers and Detection of Species Using ProbeArrays

This example shows that other non-T7 second primers, used in combinationwith a T7 promoter primer having a sequence of SEQ ID NO:11, can alsoamplify 16S rRNA sequences from a variety of Mycobacterium species. Inthese experiments, the efficiency of amplification was measured by usingan AE-labeled probe, as in Examples 1 and 2. In addition, amplifiednucleic acids from these amplification reactions were cleaved andfluorescently labeled in vitro using methods substantially as describedin PCT International Pat. App. No. PCT/FR99/01469. Then the labeledamplified nucleic acid was contacted to a GeneChip™ (Affymetrix)containing an array of sequence-specific probes that bind to sequencespresent in Mycobacterium 16S rRNA, substantially as described above(Troesch et al., 1999, J. Clin. Microbiol. 3791): 49-55). The hybridizedlabeled fragments on the probe array were washed to remove unhybridizednucleic acids and contaminants and the hybridized nucleic acids weredetected as fluorescent signal in a pattern that corresponds to thesequences of the probes on the array, referred to as “base calling.”This method was used to identify the species of Mycobacteriumrepresented by the amplified nucleic acid. Because, in these assays, thesource of the target rRNA provided was known, the percentage of correctbase calling for that target species was reported as a measure of theaccuracy of amplification and detection of the amplified nucleic acid.

The cumulative results of these tests are shown in Table 4. Theseresults show that additional combinations of primers can amplify 16SrRNA target obtained from different Mycobacterium species and theMycobacterium species can then be identified by detecting the amplifiednucleic acid on an array of probes, such that the cumulative pattern ofhybridization complexes determines the source of the target sequence.TABLE 4 % Base Non-T7 Primer Target Source RLU/copies of rRNA CallingSEQ ID NO: 16 M. tuberculosis   4 × 10⁶/500 Not tested M. tuberculosis5.7 × 10⁶/10⁴ Not tested M. intracellulare   3 × 10⁶/10⁴ Not tested M.scrofulaceum   5 × 10⁵/10⁵ Not tested M. terrae   1 × 10⁴/10⁵ Not testedSEQ ID NO: 37 M. xenopi   4 × 10⁶/10⁵ 95 M. tuberculosis   5 × 10⁶/10⁵98 SEQ ID NO: 30 M. xenopi 3.7 × 10⁶/10⁵ 97 M. tuberculosis 5.2 ×10⁶/10⁵ 99 SEQ ID NO: 29 M. xenopi   4 × 10⁶/10⁵ 88 SEQ ID NO: 28 M.xenopi 3.7 × 10⁶/10⁵ 97 SEQ ID NO: 27 M. xenopi 3.7 × 10⁶/10⁵ 97 SEQ IDNO: 31 M. xenopi   4 × 10⁶/10⁵ 94 SEQ ID NO: 32 M. xenopi 3.1 × 10⁶/10⁵90 SEQ ID NO: 33 M. xenopi 3.3 × 10⁶/10⁵ 91 SEQ ID NO: 34 M. xenopi 1.2× 10⁶/10⁵ Not tested SEQ ID NO: 24 M. xenopi 3.1 × 10⁶/10⁵ 90 SEQ ID NO:29 M. xenopi 1.1 × 10⁶/10⁵ Not tested SEQ ID NO: 21 M. celatum 2.3 ×10⁵/10⁵ 94 SEQ ID NO: 22 M. celatum 1.2 × 10⁵/10⁵ 73 SEQ ID NO: 23 M.celatum 4.4 × 10⁵/10⁵ 97 SEQ ID NO: 25 M. celatum 1.1 × 10⁶/10⁵ 78 SEQID NO: 26 M. celatum 1.3 × 10⁵/10⁵ Not tested

In separate experiments, amplification by TMA was tested by varyingamounts of target (0, 10, 100 and 1000 copies of M. tuberculosis 16SrRNA target sequence) and of enzymes used in the amplification mixture(1500 U of RT plus 2000 U T7 RNA polymerase or 2000 U each of RT and T7RNA polymerase). Amplification efficiency was monitored by detectingbinding of an AE-labeled probe as described above. Under theseconditions, the negative control (0 copies of amplicon) provided abackground level of signal (about 2000-3000 RLU), while all of thetarget-containing amplification mixtures provided significantly highersignal (4×10⁵ to 5×10⁶ RLU). For samples containing only 10 copies oftarget sequence, reaction mixtures containing 2000 U each of RT and T7RNA polymerase, provided somewhat higher detectable levels of amplifiedproduct (1.3×10⁶ RLU, mean of five reactions) than seen with thereaction mixtures containing 1500 U of RT plus 2000 U T7 RNA polymerase(4×10⁵ RLU). For samples containing 100 or 1000 copies of the targetsequence, the detectable levels of amplified products were substantiallyequivalent for both concentrations of enzyme concentrations tested(4-5×10⁶ RLU).

EXAMPLE 4 Amplification of Mycobacterium 16S rRNA Using a ModifiedPrimer

To improve the efficient of in vitro nucleic acid amplification of 16SrRNA target sequences derived from M. xenopi, a non-T7 secondamplification primer was modified to include a modified “K-base” (Lin &Brown, 1992, Nucleic Acids Res. 20: 5149-5152). Initially, the modifiedprimer was used was that of SEQ ID NO:16 in which the 25^(th) residuewas modified to be the K-base (SEQ ID NO:38) and the target was M.tuberculosis 16S rRNA. Use of this modified non-T7 primeroligonucleotide resulted in significant improvement in amplification ofM. xenopi target when 10⁶ copies of the 16S rRNA target sequence werepresent in the reaction, as shown by the results in Table 5, whichpresent the average (mean) RLU detected for amplification productsdetected as described above using an AE-labeled probe. The amplificationreactions were performed substantially as described above for each ofthe different target sequences using a combination of primers of SEQ IDNO:8 and SEQ ID NO:16 or SEQ ID NO:8 and SEQ ID NO:38, the latter beingthe primer containing the K-base modification described above. Theresults are the average of four amplification reactions for M.tuberculosis target sequences (10³ copies per reaction) and sixamplification reactions for M. xenopi target sequences (10⁶ copies perreaction). Negative controls contained water in place of target nucleicacid.

The results in Table 5 show that primers that contain modified K-baseresidues may increase in vitro amplification efficiency of a targetsequence when compared to a similar primer sequence that does notcontain a modified base. TABLE 5 Amplicons Detected (mean RLU) forDifferent Targets Using Modified or Unmodified Primers Primers: Primers:SEQ ID NO: 8 + SEQ SEQ ID NO: 8 + SEQ Target Species ID NO: 16 ID NO: 38M. tuberculosis 5.00 × 10⁶ Not Done M. xenopi 1.56 × 10⁴ 9.45 × 10⁵Negative Control  5.6 × 10³  6.0 × 10³

EXAMPLE 5 PCR Amplification Using Mycobacterium Specific Primers

This example shows the specificity of primers of the present inventionwhen used in PCR amplification and detection of the amplified DNA on asolid support having an array of immobilized probes (GeneChip™). Fortarget preparation, M. tuberculosis (ATCC 27294) and M. xenopi (ATCC19250) strains were grown in vitro using standard microbiology methods.Bacterial stock suspensions were made in water and adjusted to aconcentration of about 6×10⁸ bacteria per ml and successive dilutions inwater were made to produce a solution of 10⁴ bacteria per μl (equivalentto 104 copies of bacterial DNA per μl) which then inactivated by heatingfor 15 min at 95° C. For amplification, sterile water was used as anegative control.

PCR amplification was carried out in a microtitre 96-well plate using aindividual 45 μl reactions containing 50 mM KCl, 10 mM Tris (pH 8.3),1.5 mM MgCl2, 0.001% (wt/vol) gelatin, 5% (vol/vol) dimethylsulfoxide,0.33 μM of each primer in a pair of primers per reaction, 200 μM of eachdNTP, and 0.75 U of Taq polymerase (AmpliTaq™; Perkin-Elmer, Norwalk,Conn.) Thermal cylcing was performed in a Perkin-Elmer 9600™ thermalcycler with an initial denaturation step at 94° C. for 5 min, followedby 30 cycles of 94° C. for 1 min, 55° C. for 72° C. for 1 min, and afinal cycle of 72° C. for 10 min.

Following PCR amplification, the amplification products were analyzed byagarose gel electrophoresis, to detect the presence or absence of a bandof DNA of about 300 nt in size. No band was visible on the gel for thenegative control (water in place of target DNA) for any combination ofprimers. For the combination of primers having SEQ ID NO:11 and SEQ IDNO:16, a band of amplified DNA was seen when M. tuberculosis was thetarget but no bands was seen when M. xenopi was the target DNA provided.In contrast, when primers having SEQ ID NO:11 and SEQ ID NO:37, or SEQID NO:11 and SEQ ID NO:30 were used, no band of amplified DNA was seenwhen M. tuberculosis was the target but the expected band was seen whenM. xenopi was the target DNA provided.

Next, the amplification products of the PCR reactions were detected on asolid support having attached sequence-specific probes in atwo-dimensional array (GeneChip™), substantially as described previously(Troesch et al., 1999, J. Clin. Microbiol., 37(1):49-55, 1999). Fordetection, promoter-tagged PCR amplicons were used for generatinglabeled single-stranded RNA targets by in vitro transcription reactions(20 μl) that each contained approximately 50 ng of PCR product; 20 U ofT7 RNA polymerase (Promega); 40 mM Tris acetate (pH 8.1); 100 mMMg(acetate)₂; 10 mM dithiothreitol; 1.25 mM each of ATP, CTP, and GTP;0.5 mM UTP; and 0.25 mM fluorescein-UTP. Transcription reactions wereincubated at 37° C. for 1 hr and then the labeled RNA was hybridized tothe probe array and analyzed as described (Troesch et al., supra).

For hybridization, 5 μl the labeled RNA target was diluted in 700 μl ofhybridization buffer (0.90 M NaCl, 60 mM NaH₂ PO₄, 6 mM EDTA, pH 7.4,and 0.05% (vol/vol) Triton X-100), applied to the probe array andincubated for 30 min at 45° C. Then the probe array was washed twice in3×SSPE (0.45 M NaCl, 30 mM NaH₂ PO₄, 3 mM EDTA, pH 7.4) and 0.005%(vol/vol) Triton™ X-100 at 30° C. and the fluorescent signal emitted bylabeled RNA bound to the array was detected. The detected signalintensities (mean, median and maximum RFU), nucleotide base call (% basecall) and sequence determinations were generated by using an algorithm(GeneChip™ software, Affymetrix). A candidate selection index wasdetermined by the percentage of homology between the experimentallyderived sequence and reference sequences present on the array. Theresults are shown in Table 6. TABLE 6 Amplification Identified % BaseMean Median Maximum Primers Target DNA Species calling RFU RFU RFU SEQID NO: 11 Water None 13.5 79 71 224 SEQ ID NO: 16 (negative control) SEQID NO: 11 M. Tuberculosis M. Tuberculosis 98.4 9838 8864 26192 SEQ IDNO: 16 SEQ ID NO: 11 Water None 10.3 32 37 59 SEQ ID NO: 37 (negativecontrol) SEQ ID NO: 11 M. Xenopi M. Xenopi 94.6 13482 12055 32759 SEQ IDNO: 37 SEQ ID NO: 11 Water None 9.7 47 46 88 SEQ ID NO: 30 (negativecontrol) SEQ ID NO: 11 M. Xenopi M. Xenopi 91.9 21455 19892 45531 SEQ IDNO: 30

These results show that the amplification primers efficiently andspecifically amplified the intended target DNA. Moreover, the amplifiedsequences could be used in a probe hybidization assay to detect andidentify the source of the nucleic acid from which the amplicons wereproduced.

EXAMPLE 6 Amplification of Many Mycobacterium Species 16S rRNA SequencesUsing a Combination of Primers

This example shows the specificity of primers of the present inventionwhen used in TMA amplification and detection on a solid support havingan array of a large number of immobilized sequence-specific probes(GeneChip™). The conditions for sample preparation were substantiallythe same as described above for a typical assay except that the targetcapture solution contained 5 pmoles of SEQ ID NO:35, the washing bufferfor the particles was 10 mM HEPES, 1 mM EDTA, 150 mM NaCl and 0.1% (w/v)sodium lauryl sulfate, pH 7.5. The washed particles were resuspended in25 μl of sterile water.

The amplification conditions were as as follows. To the particles inwater were added 50 μl of amplification reagent solution (1.6 mM rUTP, 4mM rCTP, 6 mM rATP, 10 mM rGTP, 1 mM each dNTP, 80 mM Tris, 35 mM KCland 25.6 mM MgCl2) and three primers (SEQ ID NO:11, SEQ ID NO:16, SEQ IDNO:37), each at a concentration of 0.08 μM per reaction. The solutionwas mixed and covered with 200 μl of inert oil to prevent evaporation.The amplification mixture was incubated for 10 min at 60° C., then for 5min at 42° C., and 25 μl of enzyme reagent was added (2000 U of reversetranscriptase and 2000 U of T7 polymerase). The mixture was shakengently and further incubated for 1 h at 42° C.

The amplified Mycobacterium sequences were cleaved and fluorescentlylabeled as described in Example 3 and detected on a DNA probe array asdescribed in Example 6. The results are summarized in Table 7 for manyMycobacterium species (the American Type Culture Collection (ATCC,Manassas, Va., USA) source numbers are shown in parentheses followingthe species name). For each species tested, the results are show as theindentified species based on the base calling on the DNA probe chip(i.e., % correct base calling for a particular species) and the averagesignal intensity for the detected signal (mean relative fluorescenceunits or RFU) is shown. TABLE 7 Amplification and Detection of ManyMycobacterium Species Using a Single Combination of PrimersMycobacterium species Identified Species Base calling Mean RFU Abscessus(ATCC 19977) abscessus 97.8%  1702 Africanum (ATCC 25420) tuberculosis98.4% 6 519 Asiaticum (ATCC 25276) asiaticum 97.8% 4 530 avium (ATCC25291) avium 99.5%  752 bovis (ATCC 19274) tuberculosis 100.0%  4 390Celatum (ATCC 51130) celatum 96.2%  657 Celatum (ATCC 51131) celatum97.8% 4 751 Chelonae (ATCC 14472) chelonae 98.4% 2 845 Chelonaemucogenicum (ATCC 49649) chelonae 98.4%  990 Chelonae (ATCC 35752)chelonae 97.8% 2 440 Flavescens (ATCC 14474) flavescens 93.5% 2 123Fortuitum (ATCC 49403) fortuitum 97.3% 3 841 Fortuitum (ATCC 49404)fortuitum 96.2% 2 390 Fortuitum/chelonae (ATCC 6841) Fortuitum/chelonae96.2% 1 936 gastri (ATCC 15754) gastri 98.9% 3 075 Gordonae (ATCC14470)gordonae 94.1% 1 329 Haemophilum (ATCC33207) haemophilum 98.4%  874Interjectum (ATCC 51457) interjectum 98.9%  791 Intermedium (DSM 44049)intermedium 98.9% 1 022 Intracellulare (ATCC 13950) intracellulare 98.4% 741 Intracellulare (ATCC 35764) intracellulare 98.9% 2 387Intracellulare (ATCC 35770) intracellulare 95.1%  516 Kansasii (ATCC12478) kansasii 98.4% 3 170 Malmoense (ATCC 29571) malmoense 96.8% 1 076Marinum (ATCC 25039) marinum 98.9% 8 020 non-chromogenicum (ATCC 19530)Non-chromogenicum 98.4% 1 230 Paratuberculosis (ATCC 35767)Paratuberculosis 98.9% 2 716 phlei (ATCC 11758) phlei 98.9% 2 532Scrofulaceum (ATCC 19981) Scrofulaceum 99.5% 5 119 Shimoidei (ATCC27962) shimodei 94.1% 1 459 simiae (ATCC 25275) simiae 98.9% 5 392Smegmatis (ATCC 14468) smegmatis 97.3% 1 894 szulgai (ATCC 35799)szulgai 98.9%  822 terrae (ATCC 15755) terrae 98.4% 1 224 triviale (ATCC23292) triviale 98.9% 5 975 Tuberculosis (ATCC 27294) tuberculosis100.0%  3 159 Ulcerans (ATCC 19423) ulcerans 98.9% 3 177 xenopi (ATCC19250) xenopi 99.5% 2 258

These results show that a single combination of primers effectivelyamplifies 16S rRNA sequences from many Mycobacterium species, allowing arelatively simple procedure to be used to detect the presence of manydifferent species using a single assay. When combined with a detectionprocedure that uses probes specific for many species, such as a DNAprobe array present on a GeneChip™, the assay can be used to identifymany different species present in a biological sample.

The scope of the invention is defined by the claims that follow and allequivalents thereof.

1. A method of detecting Mycobacterium species present in a biologicalsample, comprising the steps of: providing a biological samplecontaining nucleic acid from at least one Mycobacterium speciescomprising a Mycobacterium 16S ribosomal RNA (rRNA) or DNA encodingMycobacterium 16S rRNA; amplifying the Mycobacterium 16S rRNA orMycobacterium DNA in an in vitro nucleic acid amplification mixturecomprising at least one polymerase activity, and a combination of atleast two primers having sequences selected from the group consisting ofa first primer of SEQ ID NO:11 and a second primer that is anoligonucleotide consisting of 19 to 25 bases containing 18 contiguousbases of SEQ ID NO:24 and three to seven bases 5′ to the 18 contiguousbases of SEQ ID NO:24 to produce amplified Mycobacterium nucleic acid;and detecting the amplified Mycobacterium nucleic acid by detecting alabel associated with the amplified Mycobacterium nucleic acid.
 2. Themethod of claim 1, further comprising in the steps of: adding to thebiological sample at least one capture oligonucleotide that specificallyhybridizes to the Mycobacterium 16S rRNA and an immobilized nucleic acidthat hybridizes to the capture oligonucleotide under hybridizingconditions to produce a hybridization complex; and separating thehybridization complex from other components of the biological samplebefore the amplifying step.
 3. The method of claim 1, wherein theamplifying step amplifies 16S rRNA or DNA encoding 16S rRNA from M.tuberculosis or a Mycobacterium other than tuberculosis (MOTT) species.4. The method of claim 1, wherein the amplifying step amplifies 16S rRNAor DNA encoding 16S rRNA from M. abscessus, M. africanum, M. asiaticum,M. avium, M. bovis, M. celatum, M. chelonae, M. flavescens, M.fortuitum, M. gastri, M. gordonae, M. haemophilum, M. intracellulare, M.interjectum, M. intermedium, M. kansasii, M. malmoense, M. marinum, M.non-chromogenicum, M. paratuberculosis, M. phlei, M. scrofulaceum, M.shimodei, M. simiae, M. smegmatis, M. szulgai, M. terrae, M. triviale,M. tuberculosis, M. ulcerans or M. xenopi.
 5. The method of claim 1,wherein the detecting step uses at least one probe that hybridizesspecifically to the amplified Mycobacterium nucleic acid.
 6. The methodof claim 5, wherein the detecting step uses at least one labeled probethat hybridizes specifically to the amplified Mycobacterium nucleicacid.
 7. The method of claim 5, wherein the detecting step uses aplurality of probes that hybridize specifically to the amplifiedMycobacterium nucleic acid.
 8. The method of claim 1, wherein theamplifying step uses a combination of at least a first primer and asecond primer, wherein the first primer is SEQ ID NO:11, and the secondprimer is selected from the group consisting of SEQ ID NO:21, SEQ NO:22,SEQ ID NO:23 and SEQ ID NO:24.
 9. The method of claim 8, wherein theamplifying step uses a combination of a first primer and a secondprimer, wherein the second primer is SEQ ID NO:21.
 10. The method ofclaim 8, wherein the amplifying step uses a combination of at least afirst primer and a second primer, wherein the second primer is SEQ IDNO:22.
 11. The method of claim 8, wherein the amplifying step uses acombination of the first primer and the second primer, wherein thesecond primer is SEQ ID NO:23.
 12. The method of claim 8, wherein theamplifying step uses a combination of the first primer and the secondprimer, wherein the second primer is SEQ ID NO:24.
 13. A composition foramplifying in an in vitro amplification reaction a Mycobacterium 16SrRNA sequence or a DNA encoding 16S rRNA, comprising a combination of atleast two oligonucleotides, wherein a first oligonucleotide contains apromoter sequence and a sequence that hybridizes to a Mycobacterium 16SrRNA or DNA sequence, and a second oligonucleotide is an oligonucleotideconsisting of 19 to 25 bases, containing 18 contiguous bases of SEQ IDNO:24 and three to seven bases 5′ to the 18 contiguous bases of SEQ IDNO:24.
 14. The composition of claim 13, wherein the compositioncomprises: at least one first oligonucleotide having the sequence of SEQID NO: 11, and at least one second oligonucleotide having the sequenceof any one of SEQ ID NO:21, SEQ ID NO:22, SEQ ID NO:23 and SEQ ID NO:24.15. The composition of claim 14, wherein the composition comprises: atleast one first oligonucleotide of SEQ ID NO:11, and at least one secondoligonucleotide of SEQ ID NO:21.
 16. A kit containing one or moreoligonucleotides having a sequence selected from the group consisting ofSEQ ID NO:21, SEQ ID NO:22, SEQ ID NO:23 and SEQ ID NO:24.
 17. The kitof claim 16, further containing an oligonucleotide of SEQ ID NO:11. 18.The kit of claim 17, containing at least one first oligonucleotide ofSEQ ID NO:11, and at least one second oligonucleotide of any one of SEQID NO:21, SEQ ID NO:22, SEQ ID NO:23 or SEQ ID NO:25.
 19. Thecomposition of claim 14, wherein the composition comprises: at least onefirst oligonucleotide of SEQ ID NO:11, and at least one secondoligonucleotide of SEQ ID NO:23.
 20. The composition of claim 14,wherein the composition comprises: at least one first oligonucleotide ofSEQ ID NO:11, and at least one second oligonucleotide of SEQ ID NO:24.